1976
DOI: 10.1016/0021-9797(76)90308-8
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Kinetics of the dehydration of calcium oxalate trihydrate crystals in aqueous solution

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Cited by 40 publications
(10 citation statements)
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“…Calcium oxalate monohydrate (whewellite) and dihydrate (weddellite) together with calcium phosphate (hydroxyapatite) are the major components of most of the urinary calculi [1,2]. Calcium oxalate trihydrate has been rarely found in kidney stones [3], but it might be important as a possible precursor in their formation [4,5].…”
Section: Introductionmentioning
confidence: 99%
“…Calcium oxalate monohydrate (whewellite) and dihydrate (weddellite) together with calcium phosphate (hydroxyapatite) are the major components of most of the urinary calculi [1,2]. Calcium oxalate trihydrate has been rarely found in kidney stones [3], but it might be important as a possible precursor in their formation [4,5].…”
Section: Introductionmentioning
confidence: 99%
“…The activation energies for the two step dehydration reactions were calculated to be 87.9 kJ mol -1 (for -2 H 2 O dehydration) and 105.3 kJ mol -1 (for -H 2 O dehydration) and the corresponding change of enthalpy was 573 and 289 J g -1 , respectively. The dehydration of COT to the thermodynamically stable monohydrate form has also been studied in aqueous solutions at various supersaturations in the temperature range of 25-40°C [35]. It has been found that the solid state nucleation and growth of COM takes place after the macroscopic growth and agglomeration of the trihydrate crystals occurs.…”
Section: Introductionmentioning
confidence: 99%
“…It has been found that the solid state nucleation and growth of COM takes place after the macroscopic growth and agglomeration of the trihydrate crystals occurs. The concluding processes probably involve solution growth and ageing of the newly formed monohydrate crystals and the overall dehydration process has an approximate activation energy of 188 kJ mol −1 [35].…”
Section: Introductionmentioning
confidence: 99%
“…Still other solvates are stable only below room temperature or have so far been found only to be metastable over the range studied. [3][4][5][6][7][8][9][10][11][12] These show that a solvate does not necessarily have to be the most stable form in its solvent at any temperature. The general trend is that hydrate stability is a function of temperature; this relationship has been alluded to in various works [13][14][15][16] and stated more clearly by Black et al 17 Based on these works, the following rule is emphasized:…”
Section: Introductionmentioning
confidence: 99%